Alkenes Flashcards

1
Q

What is the general formula for alkenes?

A

CnH2n (for aliphatic hydrocarbons).

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2
Q

What is the structure and bond angle for alkenes?

A

Planar, bond angle 120 degrees.

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3
Q

What are the two parts to a double bond?

A

The sigma bond and a pi bond.

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4
Q

How does a double bond form?

A

A sigma bond is formed directly between two carbon atoms by the overlap of orbitals. A pi bond is formed above and below the plane of the carbon atoms by sideways overlap of p-orbitals. In each carbon involved in the double bond, 3 of its electrons go into sigma bonds and 1 goes into a pi bond.

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5
Q

When an alkene reacts which bond breaks?

A

The pi bond breaks.

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6
Q

Conditions for the hydrogenation of an alkene?

A

A hydrogen gas and an alkene is passed over a finely divided nickel catalyst. The conditions are 450k and 1000kPa. This produces an saturated alkane.

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7
Q

Write the equation for the hydrogenation of ethene?

A

C2H4 + H2 —-> C2H6

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8
Q

Uses of hydrogenation?

A

Used in margarine manufacture.

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9
Q

Conditions for the halogenation of an alkene?

A

Alkenes react with halogens at room temperature. This produces a di-substituted halogenoalkane.

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10
Q

Write the equation for the halogenation of ethene with bromine?

A

C2H4 + Br2 —-> C2H4Br2

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11
Q

Conditions for the direct hydration of an alkene?

A

Steam and the gaseous alkene are heated to high temperatures (600k) and high pressures (6MPa) in the presence of a phosphoric acid catalyst. This produces an alcohol.

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12
Q

Write the equation for the direct hydration of ethene?

A

C2H4 + H2O —-> C2H5OH

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13
Q

Uses of direct hydration?

A

Used in ethanol manufacture.

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14
Q

Conditions for the electrophilic addition of an alkene?

A

Electrophiles are attracted to the pi electrons. This occurs at room temperature. A halogenoalkane is formed.

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15
Q

Write the equation for the addition of hydrogen bromide to ethene?

A

C2H4 + HBr —-> C2H5Br

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16
Q

What is the mechanism of the addition of hydrogen bromide to ethene?

A

Hydrogen bromide is a polar molecule.
(H+ - Br-). The electron pair in the pi bond is attracted to the slightly positive hydrogen atom, causing the double bond to break. A bond forms between one of the carbon atoms and the hydrogen atom. The H-Br bond breaks by heterolytic fission and Br- is formed and a carbocation is formed. The positively charged carbocation is unstable and quickly reacts with the bromide ion to form the organic product, bromoethane.

17
Q

Which way do the curly arrows point?

A

They point in the direction for which the electrons are moving.

18
Q

Addition of bromine to an alkene?

A

When the bromine approaches the alkene, the electrons in the pi bond repel the electrons in the Br-Br bond. The Br-Br is now slightly polar. The electron pair in the pi bond is attracted to the slightly positive bromine atom, which causes the double bond to break. The Br-Br bond breaks by heterolytic fission and a Br- and carbocation is formed. The positively charged carbocation is unstable and quickly reacts with the bromide ion to form the organic product.

19
Q

What to do with polymers?

A

Recycling - separate out into types.
Combustion - for energy production.
Cracking - Use as a feedstock.